Canonical Allele Identifier: PA2827881953
Gene: MITF HGNC NCBI

Linked Data

ClinVar Variation Id: 2931438
ClinVar RCV Id: RCV003785140
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341535.1:p.Gln267Arg
CA77001738
NM_001354606.2:c.800A>G